Health monitoring and diagnostic device and network-based health assessment and medical records maintenance system

ABSTRACT

A health monitoring and diagnostic device (LIFESTREAM cholesterol meter) configured as a self-contained testing and diagnostic unit in a clam-shell type case. One side of the case includes a spring-loaded finger stick and a compartment for carrying one or more packages of disposable items including a test strip, a needle for the finger stick, and an alcohol swipe. The other half of the case includes a test strip reader, a key pad, and a liquid crystal display. The meter reads a test strip carrying a droplet of blood and receives additional diagnostic information from the patient, such as age, gender, weight, and family history of heart disease. Within minutes, the meter displays test results, including total cholesterol levels. The meter also displays additional diagnostic results, such as the patient&#39;s “cardiac age,” recommended weight loss, and a cardiac risk assessment. The meter also works in connection with a network-based comprehensive health analysis and reporting system. The meter writes patient data to a smartcard. This patient data typically includes patient identification information, the test results, the diagnostic information, and the diagnostic results. A computer station reads the smartcard and establishes a network connection with a health report server over the Internet. The computer then downloads the patient data to the health report server, which prepares a comprehensive health report. Within minutes, this report is transmitted back to the computer station, where it is printed out and delivered to the patient.

REFERENCE TO RELATED APPLICATION

This application claims priority to commonly-owned U.S. ProvisionalPatent Application No. 60/107,704, filed Nov. 9, 1998; andcommonly-owned U.S. Provisional Patent Application No. 60/144,705, filedJul. 20, 1999.

TECHNICAL FIELD

This invention relates to health monitoring and diagnostic devices and,more particularly, relates to a hand-held device operable fordetermining blood lipid levels from test-strip analyses, obtainingadditional diagnostic information from a user, displaying correspondingdiagnostic results, and storing this data on a secure patient-held datacarrier, such as a smartcard. The invention also relates to a securenetwork-based health assessment and medical records maintenance systemthat receives medical information from the health monitoring anddiagnostic devices, produces health assessments based on the receivedmedical information, and stores the received medical information in asecure medical records maintenance system.

BACKGROUND OF THE INVENTION

American health care is undergoing a revolution. By the year 2000, morethan two-thirds of all American workers with health insurance will beenrolled in some kind of managed care plan, where the emphasis is onearly detection of disease and preventive care.

Fueling this revolution is the skyrocketing cost of health care,combined with new medical research showing lifestyle is important togood health. In fact, in its 1982 report on “Health and Behavior,” theNational Academy of Sciences concluded that half of the ten leadingcauses of death in the United States are primarily related to lifestyle.Dietary patterns are identified as key lifestyle choices.

Cholesterol levels are particularly important in the United States. Forthis reason, the American Heart Association, the American MedicalAssociation and the health related agencies of the U.S. government haveembarked on national education campaigns to inform the public about theimportance of making lifestyle changes to lower blood cholesterol andprevent heart disease. Although the dangers of high cholesterol havebeen widely publicized, many people fail to make effective use of thisinformation because they do not know their own blood cholesterol levels.In other words, a great many of the people with high cholesterol levelsfail to heed the advice to lower their cholesterol levels simply becausethey are unaware of their own cholesterol levels.

This situation persists because of the high cost and inconveniencepresently involved in obtaining cholesterol information. To obtain thisinformation, most people go to a physician's office, have blood drawn,and wait for the return of the blood chemistry analysis. Often,obtaining the results involves a second trip to the physician's office.This is expensive and time consuming; the average cost is about $83 foreach office cholesterol consultation, and the average wait for theresults is several days.

The cost and inconvenience involved in obtaining cholesterol testsinhibits many people from testing their cholesterol frequently enough toprovide effective positive feedback. As a result, many people who begincorrective exercise, diet, or drug therapy programs in response to highcholesterol tests often give up their corrective programs because theydo not monitor their cholesterol frequently enough to remain aware ofthe benefits of their programs. Moreover, blood cholesterol numbers bythemselves are often poor motivators for patients who feel and lookfine, and do not immediately feel or look differently when they taketheir prescriptions. In fact, studies have shown that 80% of thepatients prescribed cholesterol-lowering drug therapies stop takingtheir prescriptions within a few months. And the attrition rates forexercise and diet programs may be even higher.

In addition, there is a need for a medical records maintenance system,not only for blood cholesterol tests but for many types of medicalinformation that can be obtained outside of the hospital environment.This need will increase with increases in the availability of remotehealth monitoring devices in the future, such as blood pressuremeasuring devices, blood sugar testing devices, blood cholesteroltesting devices, AIDS testing devices, heart monitoring devices, sleeprespiration monitoring devices, reproductive cycle and pregnancymonitoring devices, epileptic and other types of seizure monitoringdevices, and a wide range of other remote health monitoring devices thatmay be developed in the future. As the availability of the remote healthmonitoring devices increases, users will have an increasing need forsecurely storing the tests results in electronic format. The currentsystem of hard-copy and electronic medical records maintained indoctors' offices will become increasingly obsolete and inconvenient asthe availability of electronically-stored medical data increases.Because a patient's medical records are highly confidential, there is aneed for a highly secure and permanent medical records maintenancesystem under the control of individual patients and their doctors.

Thus, there is a general need in the art for a less expensive and moreconvenient approach to providing cholesterol tests. There is a furtherneed for making motivational information regarding cholesterol levelsmore readily available and more effective. And there is yet another needfor a highly secure and permanent medical records maintenance systemunder the control of individual patients and their doctors.

SUMMARY OF THE INVENTION

The present invention meets the needs described above in a healthmonitoring and diagnostic device referred to as a LIFESTREAM cholesterolmeter. This meter is configured as a self-contained testing anddiagnostic unit in a clam-shell type case. One side of the case includesa biological sample gathering device, such as spring-loaded fingerstick, and a compartment for carrying one or more packages of disposableitems, typically including a test strip, a needle for the finger stick,and an alcohol swipe. The other half of the case includes a test stripreader, a user input device such as a key pad, and a display device suchas a liquid crystal display. The meter reads a test strip carrying abiological sample, such as a droplet of blood, and within minutesdisplays test results, such as total cholesterol levels, on the meter'sdisplay.

The hand-held LIFESTREAM cholesterol meter drastically reduces the costsand inconvenience associated with obtaining cholesterol tests byperforming total cholesterol tests in virtually any location, includinga physician's office, a pharmacy, a clinic, or in the privacy of thepatient's home. The meter produces the test results within minutes usingon-board circuitry and programming. The meter also includes an on-boarddiagnostic program that prompts for additional diagnostic information,such as the patient's age, gender, weight, family history of heartdisease, blood pressure, and so forth.

The meter then translates this diagnostic information, along with thetest results, into diagnostic results that may be more meaningful to theuser than the test results alone. For example, the meter may use awell-known methodology, such as the Framingham Medical Study, to producediagnostic results including the user's cardiac age (as compared tochronological age), recommended weight loss, 5-year risk of heartattack, 10-year risk of heart attack, an assessment of stroke risk, andother results that will be easily and immediately understood by thepatient. Like the test results themselves, these more meaningfuldiagnostic results are displayed on the meter within minutes.

Producing diagnostic results like “cardiac age” and “5-year risk ofheart attack” rather than total cholesterol levels alone may motivatemore people to change their lifestyles and reduce their cholesterollevels. Moreover, producing these diagnostic results instantaneously,inexpensively, and in a convenient location encourages frequent testingand provides patients with the positive feedback necessary to encouragecontinued compliance with drug therapies and lifestyle changes.Ultimately, widespread use of the LIFESTREAM cholesterol meter can beexpected to improve cardiac health nationwide, shift the focus ofcardiac treatment from corrective to preventative, improve the cardiachealth of the population in general, and reduce medical costs and healthinsurance rates.

The benefits of the LIFESTREAM cholesterol meter may be improved overtime and extended to other health problems because the meter isprogrammable and configured to perform multiple types of tests. That is,although the meter will be initially configured to perform totalcholesterol tests using test strips and human blood samples, it is alsoconfigured to perform multiple types of tests using different types oftest strips or other test media carrying other types of biological fluidor tissue samples. For example, the meter may also produce other typesof blood lipid test results, such as HDL cholesterol, triglycerides, LDLcholesterol, etc. The meter may also perform other types of tests, suchas blood glucose tests, AIDS tests, cancer tests, and virtually anyother type of test that can be performed using a test strip or anothersuitable test medium carrying a sample of biological fluid or tissue. Toaccommodate multiple tests, the meter typically includes four romkeysockets that allow the meter to carry and read four different romkeys.

The LIFESTREAM cholesterol meter also works in connection with anetwork-based comprehensive health analysis and reporting system. Themeter includes a data drive that writes patient data stored within themeter to a patient-held data storage device, such as a smartcard. Thispatient data typically includes patient identification information, thetest results, the diagnostic information, and the diagnostic results. Acomputer station, such as a typical desktop or laptop personal computer,can then read the smartcard and establish a network connection with ahealth report server, typically over the Internet. The computer thendownloads the patient data to the health report server, which prepares acomprehensive health report. This report is then transmitted back to thecomputer station, where it is printed out and delivered to the patient.

The health report server typically works in concert with the patient'sphysician or pharmacist, who may provide additional diagnosticinformation to the server, such as a newly-prescribed drug therapy,other currently-prescribed drugs for the patient, exercise and dietaryrecommendations, and so forth. Within minutes, the health report serverassembles a comprehensive health report including a data sheet for thenewly-prescribed drug, cross-reaction information for thenewly-prescribed drug and the other currently-prescribed drugs, weightand total cholesterol goals, exercise and dietary recommendations, anyfood or activity warnings associated with the overall therapy package,and recommendations for on-going monitoring using the meter. Thisprovides a complete written record of the patient's current condition,the therapy prescribed by the physician and filled by the pharmacist,and a roadmap for monitoring the patient's progress during the ensuingtherapy.

The comprehensive health report may also include additionalpatient-specific information, such as the diagnostic information andresults compiled by the meter, and additional diagnostic and healthassessment information compiled by the server. For example, the reportmay include a trend analysis showing how cholesterol, blood glucose, andweight levels have changed over multiple readings. The report may alsoinclude generally-applicable educational information, such as coronaryrisk factors, dietary guidelines for reducing cholesterol levels,diabetes information, cancer information, and the like. At present, apatient may have to undergo a physical examination, pay thousands ofdollars, and wait weeks to obtain a similar comprehensive health report.The network-based comprehensive health analysis and reporting system,working in concert with the LIFESTREAM cholesterol meter, allows thepatient to obtain the report within minutes at a fraction of the cost.

The meter also includes a number of advantageous security features. Forexample, the meter cannot be activated until a user enters a properactivation code. This typically requires that the user call themanufacturer, which provides an opportunity to verify the meter'sauthenticity, set up a data file for the meter in the health reportserver, and tell the user how to update the meter software, ifnecessary. If a software update is indicated, the user may be instructedto activate the meter, initialize a smartcard, load the smartcard into acomputer station, and establish a network connection with the healthreport server. The server can then download the new software (e.g., newversion of an existing software module or a new software module) to thesmartcard, which, in turn, can be placed back in the meter. The newsoftware can then be uploaded to the meter.

The meter may also require validation of all test strips. Validation isimportant for some types of tests because readings obtained from eachtest strip will have to be interpreted correctly to obtain correct testresults, and the calibration data used to interpret the readings fromdifferent lots of test strips may vary significantly. To allow propercalibration, each lot of test strips has a corresponding memory device,such as a romkey, that must be placed into the meter. The romkeyincludes a code number, an expiration date, and the calibration data forinterpreting readings from the corresponding test strips. A test stripidentification number that is mathematically derived from the codenumber is printed on the test strips or their packaging. The user mustenter the proper test strip identification number into the meter, whichthe meter verifies with reference to the code number and the expirationdate read from the romkey. This allows the meter to prevent the use ofexpired test strips and to also prevent test strips from being used incombination with incorrect romkeys.

Test strip validation is also an important aspect of one business modelfor deploying the meters. That is, the meters themselves may be providedfor use at little or no charge to individual patients, whereasproprietary test strips will be sold to generate revenue from use of themeter. This may be a desirable business model for deploying the devicesbecause it minimizes the initial cost that an individual patient mustpay to begin using the device. Having to sell each device at its fullcost, on the other hand, would undermine the economic feasibility ofusing the device in many contexts. For this business model, the metershould only activate for use with proprietary test strips aftervalidation of the test strips.

The meter may also require each smartcard to be initialized with apersonal identification number (PIN). Patient-specific PINs allowmultiple patients to use the same meter, and also allows each patient'sdata to be secure to that patient. That is, only the patient or someoneauthorized by the patient (i.e., knowing the patient's PIN) can read themedical data stored on the smartcard. In this manner, each patientcontrols his or her own medical data, which can be a particularlyimportant attribute for highly sensitive medical data, such as AIDStests, cancer tests, and the like.

Generally described, the invention provides a test strip for use with ahealth monitoring device or meter. The test strip, when carrying asample of biological fluid or tissue, may be read by the meter to obtaintest results based on the sample and calibration data specific to thetest strip. The test strip also corresponds to a memory device thatstores a code number and the calibration data, which may also be read bythe meter. The test strip has an associated test strip identificationnumber that is mathematically derived from the code number and printedon the test strips, the packaging for the test strips, or a tag packagedwith the test strips.

To verify test strips, the meter reads the code number from the memorydevice, mathematically derives a test strip identification numbercorresponding to the code number, compares the received test stripidentification number to the derived test strip identification number,and activates the meter for use with the test strip only if the receivedtest strip identification number corresponds to the derived test stripidentification number.

The memory device may also store an expiration date for the test strip,which may be read by the meter. In this case, the meter may activate foruse with the test strip only if the expiration date is prior to acurrent date read by the meter from an internal clock. The memory devicemay be a romkey that is inserted into a socket housed within the meter.The romkey is typically packaged with an associated group of the teststrips, and the test strip identification number is typically printed onthe test strips, printed on packaging for the test strips, or printed ona tag packaged with the test strip.

The invention also provides a hand-held health monitoring device ormeter that includes an enclosure for housing a disposable test strip foruse with the meter. The meter also includes a holder for removablysupporting a device for gathering a sample of biological fluid ortissue, such as a finger stick. The meter also includes a test stripreader operable for reading the test strip carrying the sample ofbiological fluid or tissue and obtaining test results based on thesample and calibration data specific to the test strip. A memory readingdevice (e.g., romkey socket) functionally connected to the test stripreader reads the calibration data from a memory device (e.g., romkey). Auser input device, such as a key pad, receives user input commands and adisplay device, such as a liquid crystal display, displays informationon the meter.

The meter also includes a processor that is functionally connected tothe test strip reader, the user input device, and the display device.The processor contains a program module that obtains the test resultsfrom the test strip reader and causes the display device to display thetest results. A data drive functionally connected to the processorwrites the test results to a removable memory storage device, such as asmartcard. The meter may be packaged in a clam-shell case that opens toreveal first and second compartments. The first compartment may containthe enclosure for housing the disposable test strip and the holder forremovably supporting the biological fluid or tissue gathering device,and the second compartment may contain the test strip reader, the memoryreading device, the display device, the processor, and the data drive.

To provide activation verification, the meter may receive an activationcode through the user input device, compute an activation code based onthe current date and instructions contained in an activation routinestored within the meter, and activate the meter only if the computedactivation code corresponds to the received activation code. Inaddition, to provide security to a patient's medical data, the meter maydetermine whether a PIN has been previously stored on the removablememory storage device. If a PIN has not been previously stored on theremovable memory storage device, the meter prompts the user to enter aPIN and stores the received PIN on the removable memory storage device.Alternatively, if a PIN has been previously stored on the removablememory storage device, the meter prompts the user to enter a PIN,compares the stored PIN to the received PIN, and writes the test resultsto the removable memory storage device only if the stored PINcorresponds to the received PIN.

The test strip reader may also be operable for reading a second type oftest strip carrying a second sample of biological fluid or tissue andobtaining health-related test results based on the second sample ofbiological tissue or fluid and calibration data specific to the secondtype of test strip. In this case, the meter may include a second memoryreading device (e.g., romkey socket) functionally connected to the teststrip reader and operable for reading calibration data from a secondmemory device (e.g., romkey) corresponding to the second type of teststrip. For example, the meter may read both blood lipid test strips andblood glucose test strips. As noted previously, the meter typicallyincludes four romkey sockets that allow the meter to carry and read fourdifferent romkeys.

The meter may also prompt the user to enter diagnostic information usingthe user input device, such as gender, ethnicity, family history ofheart disease, personal history of heart disease, personal history ofdiabetes, personal history of smoking, height, weight, age, bloodpressure, and fitness level. The meter may then perform a diagnosticanalysis and produce diagnostic results based on the test results anddiagnostic information, and display diagnostic results. For example, thediagnostic results may include a medical risk index, a recommendedweight loss, a five-year risk of heart attack, a ten-year risk of heartattack, a cardiac age, an extended age, and a risk of stroke.

The invention also provides a system for remotely producing healthreports. This system includes a health monitoring device or meter, asdescribed above, a computer station, and a health report serverconnected with the computer station through a network, such as theInternet. The meter writes health-related test results to a memorystorage device. The computer station reads the test results from thememory storage device, establishes a network connection with the healthreport server, receives additional diagnostic information from a user,and transmits the test results and the additional diagnostic informationto the health report server. The server, in turn, compiles a healthreport based on the test results and the additional diagnosticinformation and transmits the health report to the computer station,where the report may be printed and delivered to the patient.

The health report may include a trend analysis with test resultscompiled for a number of samples, such as total cholesterol level andblood glucose level trend reports. The additional diagnostic informationmay include a newly-prescribed drug and other currently-prescribeddrugs, and the health report may include a data sheet for thenewly-prescribed drug and information relating to cross-reactionsbetween the newly-prescribed drug and the other currently-prescribeddrugs. The health report may also include a target weight and totalcholesterol levels, a schedule for future testing using the meter,health assessment summary, a coronary risk assessment, dietaryguidelines to lower cholesterol, and other educational information.

The business model described above is largely dependent on the sale ofproprietary test strips for the collection of revenue from end users.That is, the health monitoring device itself may be made available toindividual patients at little or no cost, with the sale of proprietarytest strips providing a major source of revenue for the proprietor ofthe health monitoring device. As noted previously, this may be adesirable business model for deploying the devices because it minimizesthe initial cost that an individual patient must pay to begin using thedevice. Having to sell each device at its full cost, on the other hand,would undermine the economic feasibility of using the device in manycontexts.

Nevertheless, it may also be desirable to provide a health monitoringdevice that does not rely on the sale of proprietary test strips as amajor source of revenue. For example, the health monitoring device maybe adapted to read non-proprietary test strips, or may incorporate areusable and/or non-invasive testing device, such as an electrode, bloodpressure monitoring device, sonic testing device, thermometer, salivatesting device, optical testing device, and the like. Of course, anon-invasive multi-use testing device may be used many times withoutaffording the proprietor of the health monitoring device an opportunitycollect revenue associated with each use of the device.

To provide an opportunity for the proprietor of the health monitoringdevice to collect revenue based on use of the device, the removablememory storage device may be utilized as a type of “debit card” orpayment source for use with the health monitoring device. That is, theremovable memory storage device may be purchased with a monetary value,or it may have a monetary value that is replenishable over the Internetusing a bank credit or debit card or other conventional payment source.The health monitoring device may then deduct the cost of performingparticular services from the monetary value represented by the monetarybalance stored on the removable memory storage device. In other words,the health monitoring device may be configured to activate for theperformance of a service upon deducting a charge for the service from amonetary value stored on a removable memory storage device inserted intothe device.

This business model includes a health monitoring device operable forobtaining medical data associated with a patient and reading an initialmonetary balance stored on a removable memory storage device. The healthmonitoring device determines whether the initial monetary balance issufficient to pay a monetary value assigned to performance of a testinvolving the medical data to be performed by the testing device. If theinitial monetary balance is sufficient to pay for the test, the healthmonitoring device computes a revised monetary balance by deducting themonetary value assigned to performance of the test from the initialmonetary balance, replaces the initial monetary balance with the revisedmonetary balance on the removable memory storage device, and activatesthe health monitoring device for performance of the specified service.

The business model also includes a system that includes one or more ofthe health monitoring devices described above, one or more removablememory storage devices, and a network-based server operable for remotelycharging a cost to a payment source and crediting the cost to an initialbalance stored on the removable memory storage device. The network-basedserver may also remotely store the monetary value assigned toperformance of the test on the removable memory storage device. In thiscase, the health monitoring device reads the monetary value assigned toperformance of the test from the removable memory storage device. Thus,rate schedules for various services to be performed by the healthmonitoring device may be changed from time to time, based on quantitydiscounts or other considerations.

The invention also includes a secure medical records maintenance system.Although this system is specifically adapted for use with the healthmonitoring device described above, it may be used to store any type ofelectronic data including a wide variety of medical records, and isparticularly convenient for storing a wide range of electronic medicaldata generated remotely from the hospital or doctor's officeenvironment. The secure medical records maintenance system includes anumber of removable memory storage devices, which are each operable forstoring medical data for an associated patient. Each removable memorystorage device also stores a patient-specified personal identificationnumber (PIN), a medical records identification number secured by thePIN, and a patient identification number secured by the PIN.

The data stored on the removable memory storage device is downloadableto a two-server system including a first remote server that storespatient identification information indexed by patient identificationnumbers, and a second remote server that stores patient medical dataindexed by the medical records identification number. For securitypurposes, the medical data maintained in the second remote server cannotbe correlated to the associated patient identification informationmaintained in the first remote server based on the information containedin the first and second remote servers.

To allow correlation of the data stored in the two servers, the securemedical records maintenance system includes a correlation table uniquelyassociating each medical records identification number with a particularone of the patient identification numbers. The correlation table for aparticular patient typically resides on the patient's removable memorystorage device. The correlation table for a practitioner's patients mayalso reside on the practitioner's computer, such as a doctor's orpharmacist's computer, that is associated with a licensed medicalpractitioner having an assigned professional registration number. Forfurther security, the first and second remote servers are accessed bythe practitioner's computer through encrypted communications secured byan application procedure that includes validation of the practitioner'sregistration number. The application procedure may be further secured byreceipt and validation of a practitioner-supplied PIN. Moreover, theapplication procedure typically includes issuance of a clientcertificate insuring that access to the first and second remote serversoccurs from the same practitioner's computer and browser that initiatedthe application procedure.

Because the data on the servers is separate and secure from each other,access may be granted to either server without identifying anyparticular patient's medical data. For example, access may be granted tothe first remote server, but not to the second server, for the purposeof generating a mailing list of patients without divulging any medicaldata associated with the patients. Similarly, access may be granted tothe second remote server, but not to the first server, for the purposeof conducting investigative analyses involving the medical data withoutdivulging any patient identification information associated with thepatients.

For further data security and because each removable memory storagedevice only has a limited data storage capability, the medical datastored on each removable memory storage device may be automaticallyerased from the memory storage device after the data is entered into thesecond remote server. To obtain the medical data, the removable memorystorage device is receivable within a hand-held health monitoring deviceoperable for storing the medical data on the removable memory storagedevice. And to download the medical data to the medical recordsmaintenance system, the removable memory storage device is receivablewithin a computer operable for reading the medical data and transmittingit to the second remote server over the Internet.

That the invention improves over the drawbacks of health monitoring anddiagnostic systems and accomplishes the advantages described above willbecome apparent from the following detailed description of the exemplaryembodiments and the appended drawings and claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a front view of a hand-held health monitoring and diagnosticdevice in an open position.

FIG. 1B is a rear view of the hand-held health monitoring and diagnosticdevice of FIG. 1 in an open position.

FIG. 2 is a block diagram illustrating a system for remotely producinghealth reports.

FIG. 3 is a functional block diagram of a health monitoring anddiagnostic device.

FIG. 4 is a logic flow diagram illustrating a routine for activating ahealth monitoring and diagnostic device.

FIG. 5 is a logic flow diagram illustrating a routine for computing anactivation code for a health monitoring and diagnostic device.

FIG. 6 is a logic flow diagram illustrating a routine for verifying atest strip for a health monitoring and diagnostic device.

FIG. 7 is a logic flow diagram illustrating a routine for computing atest strip identification number for a health monitoring and diagnosticdevice.

FIG. 8 is a logic flow diagram illustrating a routine for enteringdiagnostic program modules into a health monitoring and diagnosticdevice.

FIG. 9 is a logic flow diagram illustrating a routine for computingimmediate diagnostic results in a health monitoring and diagnosticdevice, and for remotely producing health reports.

FIG. 10 is a logic flow diagram illustrating a routine for obtainingcholesterol-related diagnostic information for a health monitoring anddiagnostic device.

FIG. 11 is a logic flow diagram illustrating a routine for computingimmediate cholesterol-related diagnostic results for a health monitoringand diagnostic device.

FIG. 12 is a logic flow diagram illustrating a routine for remotelyproducing health reports.

FIG. 13 is a logic flow diagram illustrating a routine for savingmedical data to a PIN-secured removable memory storage device for ahealth monitoring and diagnostic device.

FIG. 14 is a functional block diagram of a system for using a healthmonitoring and diagnostic device in connection with a secure medicalrecords maintenance system.

FIG. 15 is software architecture diagram illustrating a system forconducting secure communications between a health monitoring anddiagnostic device and a secure medical records maintenance system.

FIG. 16 a functional block diagram illustrating security aspects of asecure medical records maintenance system.

FIG. 17 is a logic flow diagram illustrating a process for acommunicating with a secure medical records maintenance system.

FIG. 18 is a logic flow diagram illustrating a process for applying foraccess to a secure medical records maintenance system.

FIG. 19 is a logic flow diagram illustrating a process for logging intoa secure medical records maintenance system.

FIG. 20 is an illustration of a “switchboard” user interface in a securemedical records maintenance system.

FIG. 21 is an illustration of an “address” user interface in a securemedical records maintenance system.

FIG. 22 is an illustration of a “billing information” user interface ina secure medical records maintenance system.

FIG. 23 is an illustration of a “cover letter” user interface in asecure medical records maintenance system.

FIG. 24 is an illustration of a “patient selection” user interface in asecure medical records maintenance system.

FIG. 25 is an illustration of a “patient information” user interface ina secure medical records maintenance system.

FIG. 26 is an illustration of a “questionnaire data” user interface in asecure medical records maintenance system.

FIG. 27 is an illustration of a “generate reports” user interface in asecure medical records maintenance system.

FIG. 28 is an illustration of typical health assessment charts generatedby a secure medical records maintenance system.

FIG. 29 is an illustration of an additional health assessment chartgenerated by a secure medical records maintenance system.

FIG. 30 is a logic flow diagram illustrating a routine for adding amonetary value to a smartcard for use with a health monitoring device.

FIG. 31 is a logic flow diagram illustrating a routine for using asmartcard to pay for a service provided by a health monitoring device.

DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION

Hand-Held Health Monitoring and Diagnostic Device

Turning now to the figures, in which like numerals refer to likeelements through the several figures, FIG. 1A is a front view of ahand-held health monitoring and diagnostic device 10, which is alsoreferred to as a meter or a LIFESTREAM cholesterol meter. The meter 10is housed in a clam-shell case 12 including a first compartment 14 and asecond compartment 16. The case 12 may be opened, as shown in FIG. 1A,or closed about a hinge 18. This allows a patient to close the meter 10for transportation or storage, and then easily open it for use. When inuse, the patient may place the meter 10 in the open position on a flatsurface, such as a table or seat, or hold the meter by hand.

Although the meter 10 is shown in a hinged clam-shell, hand-heldconfiguration, it could alternatively be embodied in otherconfigurations, such wall-mounted, built into a movable cart, built intoa desktop computer, built into a fixed podium, and so forth. Inaddition, the hinged clam-shell case could be replaced by a non-hingedcase, a separable multi-piece case, a case with a pull-out drawer, acase with a flat cover, a meter that fits into a separate zippered case,and other types of single- or multi-piece configurations. Many othervariations of the meter case configuration will be apparent to thoseskilled in the art.

The first compartment 14 includes a holder 18 for removably supporting abiological sample gathering device, in this instance a conventionalspring-loaded finger stick 20. Although the holder 18 is shown as a clipwith two arms that fit snugly against the finger stick 20, the holdermay have any other configuration suitable for removably supporting thefinger stick, such as a channel into which a pencil-like finger stick isinserted, an openable enclosure, snaps, a VELCRO fastener, and the like.If samples other than blood are to be gathered, the first compartment 14could alternatively house other types of biological sample gatheringdevices, such as a skin sample collector, a saliva collector, a stoolsample collector, and so forth. In addition, the meter 10 may includeother types of instruments for gathering test data, for example themeter may be adapted to read non-proprietary test strips, or mayincorporate a reusable and/or non-invasive testing device, such as anelectrode, blood pressure monitoring device, sonic testing device,thermometer, saliva testing device, optical testing device, and thelike.

The first compartment 14 also includes an openable enclosure 24 forstoring one or more packages 26 of disposable items. Specifically, eachpackage may contain a test strip 28, a needle 29 for the finger stick20, and an alcohol swipe 30. These disposable items are tailored forone-time use with the finger stick 20. If the meter 10 includesbiological sample gathering devices other than the finger stick 20,other types of disposable items may be stored in the enclosure 24. Inaddition, the enclosure 24 may have other configurations suitable forstoring or holding disposable items, such as a drawer, a tiltingchannel, a clip, and so forth.

The second compartment 16 houses the electronic components of the meter10, including a test strip reader 32, a display device 34, a user inputdevice 36, and one or more memory reading devices 38 a-d. Each of thesememory reading devices is configured to receive a corresponding memorydevice 40 a-d. The second compartment 16 also includes an instructionallabel 42 located adjacent to the display device 34. Internally, thesecond compartment 16 houses a motherboard, an analyzer board, and adata drive that control the functionality of the meter 10. Theseinternal components are described with reference to FIG. 3, and thefunctionality of the meter 10 is described with reference to FIGS. 4-13.Additional functionality of the meter 10 for use with a debit-card typepayment system is described with reference to FIGS. 30-31.

The test strip reader 32 may be a GLUCOTREND Basic TIM (test instrumentmodule) assembly No. 1739905-741 manufactured by Boehringer Mannheim,Roche Diagnostics GmbH. This is a commercially-available optical teststrip reader suitable for reading chemical test strips carrying humanblood samples and producing either blood glucose readings, totalcholesterol readings, or both. Alternatively, other suitable types oftest strip readers may be included in the meter 10, and multiple teststrip readers may be included in the meter, if appropriate. This may bedesirable, for instance, if biological samples other than blood are tobe analyzed by the meter. The meter 10 may be configured with additionalreusable and/or non-invasive testing devices, such as an electrode,blood pressure monitoring device, sonic testing device, thermometer,saliva testing device, optical testing device, and the like.

The display device 34 may be a conventional liquid crystal display (LCD)configured to display at least two lines of text including at least 14characters per line. This visual display works in concert with a speaker35 that beeps to convey audible messages. The speaker may also produceother types of audible messages, such as tones, recorded messages, asimulated human voice, and the like. The meter 10 may also include othertypes of visual display devices, such as an electronic capacitivematrix, a small video display, or other types of suitable visual displaydevices. The meter 10 may also include a jack for connecting the meterto external display devices, such as a computer monitor or videodisplay.

The user input device 36 may be a keypad with a first key section 44 anda second key section 46. The first key section 44 includes four keys, a“scroll” key, a “yes” key, a “no” key and an “enter” key. The second keysection 46 includes twelve keys, including ten numerical keys, a “clear”key, and an “on/off” key. The user input device 36 may include other keypatterns and other types of user input devices, such as atouch-sensitive screen, a voice-recognition device, or other inputdevices. The meter 10 may also include a jack for connecting the meterto external input devices, such as a keyboard or joystick.

The memory reading devices 38 a-d may be romkey sockets, and the memorydevices 40 a-d may be romkeys that removably insert into the sockets. Asshown in FIG. 1A, the meter 10 preferably includes four romkey sockets.Nevertheless, the meter 10 could also be configured with only one socketbecause the romkeys themselves are removable. The romkeys, which storeidentification, expiration, and calibration data for a corresponding lotof test strips 28, are desirable because they are small, may be easilypackaged with the corresponding test strips, and have an adequate amountof computer-readable memory. But the romkey sockets may be replaced by amagnetic card reader, an optical reader, or another reader suitable foruse with a memory storage device that can be easily shipped with acorresponding lot of test strips 28 and has an adequate amount ofcomputer-readable memory.

The instructional label 42 located adjacent to the display device 34typically includes instructions for entering diagnostic information intothe meter 10. This label may also include instructions for using themeter 10 in concert with a remote health report system, which isdescribed with reference to FIG. 2. As this type of information may beunderstood best when explained by a physician or pharmacist, theinstructional label 42 may be included on meters provided to physiciansand pharmacists, but may be excluded from meters provided for home useby individual patients. The programmed functionality of the meter mayalso be adjusted accordingly.

To use the meter 10, a patient first opens the meter and removes thefinger stick 20 and the package of disposable items 26. The patient thenopens the package, installs the needle 29 in the finger stick 20, andwipes the alcohol swipe 30 on the area of the finger to be stuck withthe needle. The patient also inserts the correct romkey for the teststrip 28, represented by the romkey 40 d, into a corresponding romkeysocket 38 d and manipulates the keypad 44, 46 to indicate to the meter10 which romkey socket contains the correct romkey. The patient thensticks the selected finger with the finger stick 20, places a droplet ofblood 44 on an indicated area of the test strip 28, and inserts the teststrip 28 into the test strip reader 32.

The user then manipulates the input device 36 by following promptsdisplayed on the display device 34 to complete the test. Within minutes,the meter 10 completes the test and displays the test results, such astotal cholesterol levels, blood glucose levels or another testingservice provided by the meter, on the display device 34. If appropriate,the user may also manipulate the input device 36 to enter additionaldiagnostic information into the meter, such as gender, ethnicity, familyhistory of heart disease, personal history of heart disease, personalhistory of diabetes, personal history of smoking, height, weight, age,blood pressure, and fitness level. Within minutes, the meter 10 performsa diagnostic analysis and produces diagnostic results, such as a medicalrisk index, a recommended weight loss, a five-year risk of heart attack,a ten-year risk of heart attack, a cardiac age, an extended age, and arisk of stroke. These diagnostic results are also immediately displayedon the display device 34.

For a blood lipid or cholesterol test, the well-known Framingham MedicalStudy may provide the methodology used by the meter 10 to produce thediagnostic results from the test results and the diagnostic information.Other methodologies, such as those sanctioned by the NationalCholesterol Education Program, the American Heart Association, theAmerican Medical Association, or another appropriate organization mayalso be used. In fact, the meter 10 may allow the user to select amongseveral alternative diagnostic program modules stored within the meter.These diagnostic program modules may be updated from time to time, andnew diagnostic program modules may be added to the meter 10 through thedata drive, which is described below.

FIG. 1B is a rear view of the meter 10, which shows the outside of themeter. The outside of the first compartment 14 includes themanufacturer's name, Lifestream Technologies, Inc., and the meter'strademark, LIFESTREAM. The outside of the second compartment 16 includesa data drive 50, which includes an opening 52 for receiving a removablememory storage device 54. For example, the data drive 50 may be asmartcard drive, such as an STM IC: MC33560ADW manufactured by Motorola,and the removable memory storage device 54 may be a smartcard usablewith this drive. This smartcard typically includes an electrical contact56 for reading and writing data and a small microprocessor 58, whichtypically controls security aspects of the smartcard. Specifically, thesmartcard includes a PIN-protected secure memory and an unsecure memory.The microprocessor 58 controls the PIN and any other functionalityresident on the smartcard.

The smartcard is an advantageous memory storage device because of itssmall size, its on-card PIN security feature, and its on-boardprogrammable processing unit. Moreover, it is expected that smartcardswill become increasingly popular in the near future, and most personalcomputers will come with factory-installed smartcard drives.Nevertheless, the meter 10 could include other types of data drives,such as a floppy disk drive, an optical disk drive, a removable RAMchip, or any other suitable type of removable memory storage device.Furthermore, the meter 10 could also include a wire-line data port forconnecting a cable or another computer station in addition to or as analternative to the data drive. Similarly, the wire-line data port couldbe replaced by a wireless communication device, such as aradio-frequency link, a laser link, an infra-red link, and so forth.

The second compartment 16 also includes a battery enclosure 60 housing aremovable battery 62 for powering the meter 10. The battery 60, whichmay be a disposable 9 Volt battery, may be replaced or augmented by anA/C power cord and an appropriate power inverter. The battery 60 also bereplaced by a rechargeable battery augmented with a battery charger thatmay be located within the meter 10 or in a separate enclosure, such as astorage container for housing the meter when it is not in use.

Remote Health Report System

FIG. 2 is a block diagram illustrating a system 100 for remotelyproducing health reports. The PIN-securable smartcard described aboveallows multiple patients to use the same meter, and also allows eachpatient to control access to his or her medical data. The smartcard istypically used as a temporary storage location for one or several testresults. From time to time, each patient is expected to download themedical data contained on his or her smartcard to a health report server102 for permanent storage. The smartcard is then erased (except for thePIN and any other security information contained in the secure memory),which frees the memory space for new medical data. The smartcard mayalso be used to receive new program modules or new versions of programmodules from the health report server 102 and upload these programmodules to the meter 10.

The system 100 includes the meter 10, which downloads medical data tothe removable memory storage device 54. This medical data typicallyincludes patient identification information, test results generated bythe meter, diagnostic information entered into the meter 10 by thepatient, and the diagnostic results 104 computed by the meter andimmediately displayed on the meter at the time of the test. If theremovable memory storage device 54 is a smartcard, it may then be placedin a converter, such as a conventional smartcard-to-floppy-diskconverter 106, which can be directly inserted into a computer station108. The converter 106 will be unnecessary, of course, if the computerstation 108 includes a smartcard drive, or if another communicationmechanism is employed to transmit information between the computerstation 108 and the meter 10.

Once the medical data arrives at the computer station 108, itestablishes a network connection with the health report server 102,typically over the Internet 110. The medical data is then transmitted tothe health report server 102, which may also prompt the user foradditional diagnostic and health report information. Specifically, thehealth report server 102 typically works in concert with the patient'sphysician or pharmacist, who may provide additional diagnosticinformation to the server, such as a newly-prescribed drug therapy,other currently-prescribed drugs for the patient, exercise and dietaryrecommendations, and so forth. Within minutes, the health report server102 assembles a comprehensive health report 112 that is transmitted backto the computer station 108, where it may be printed on a local printer114. User access procedures and a menu-driven user interface system forgenerating the health reports is described with reference to FIGS.17-29.

The comprehensive health report 112 typically includes a data sheet forthe newly-prescribed drug, cross-reaction information for thenewly-prescribed drug and the other currently-prescribed drugs, weightand total cholesterol goals, exercise and dietary recommendations, anyfood or activity warnings associated with the overall therapy package,and recommendations for on-going monitoring using the meter. Thisprovides a complete written record of the patient's current condition,the therapy prescribed by the physician and filled by the pharmacist,and a roadmap for monitoring the patient's progress during the ensuingtherapy.

The comprehensive health report may also include additionalpatient-specific information, such as the diagnostic information andresults compiled by the meter, and additional diagnostic and healthassessment information compiled by the server. For example, the reportmay include a trend analysis showing how blood lipid, blood glucose, andweight levels have changed over multiple readings. The report may alsoinclude generally-applicable educational information, such as coronaryrisk factors, dietary guidelines for reducing cholesterol levels,diabetes information, cancer information, and the like. At present, apatient may have to undergo a physical examination, pay thousands ofdollars, and wait weeks to obtain a similar comprehensive health report.The network-based comprehensive health analysis and reporting system,working in concert with the LIFESTREAM cholesterol meter, allows thepatient to obtain the report within minutes at a fraction of the cost.

The Internet 10 allows a wide variety of users to access the healthreport server 102, which allows meters to be deployed in a variety ofsettings. For example, the accessing computer stations may include aphysician's computer station 116, a pharmacist's computer station 118,an individual's computer station 120, and many others. This will allowmeters to be effectively deployed for multi-patient use in clinics,physicians' offices and pharmacies, as well as for individual patient orfamily use in the privacy of their own homes.

Functional Operation of the Meter

FIG. 3 is a functional block diagram of the health monitoring anddiagnostic device 10, which is also referred to as a meter. The meterincludes an analyzer board 150, a mother board 152, a memory readingdevice 154 including the romkey sockets 38 a-d and corresponding romkeys40 a-d, and a user interface 156 including the display device 34, thespeaker 35, and the input device 36. The memory reading device 154 andthe user interface 156 were described with reference to FIG. 1A.Although the analyzer board 150 and the mother board 152 may beconfigured as two separate integrated circuit boards, alternatively theymay be combined into a single integrated circuit board, or deployed onmore than two integrated circuit boards.

The analyzer board 150 may be part of the GLUCOTREND Basic TIM (testinstrument module) assembly No. 1739905-741 manufactured by BoehringerMannheim, Roche Diagnostics GmbH. This board includes the test stripreader 32, which was described with reference to FIG. 1A, a testinstrument module 158, and a romkey driver 160. The test strip reader 32reads the test strip 28 carrying the blood sample 44. The romkey driver160 reads the calibration data for the test strip 28 from acorresponding romkey, such as the romkey 40 d, and the test instrumentmodule 158 computes the test results from the test strip reading and thecalibration data. These test results are then passed to the motherboard152.

The motherboard 152 includes a non-interruptible battery 162, such as alithium battery. The non-interruptible battery 162, which powers theon-board clock 164, is distinct from the power supply battery 62 (shownon FIG. 1B). The additional non-interruptible battery 162 allows theclock to continue functioning even when the power supply battery 62 runsdown or is removed from the meter 10. The motherboard 152 also includesa processor 166 and a memory 168 that control the functionality of themeter 10. Specifically, the memory 168 stores and the processor 166implements a meter activation routine, test strip verification routine,diagnostic routines, and a read/write security routine. These programmodules are described with reference to FIGS. 4-13. The motherboard 152also includes a data drive 170 that reads data from and writes data tothe removable data storage device 54, such as a smartcard.

The mother board processor 166 may be a 40-pin DIP CPU Model No.MC68HC705C9ACP manufactured by Motorola. The data drive 170 may be a STMIC Model No. MC33560ADW ISO read/control card manufactured by Motorola,supported by an ISO Card Socket, Model No. 145206-3 physical interfacemanufactured by AMP. However, any of these specific devices may bereplaced by equivalent devices capable of performing the functionalityof the meter 10 described in this specification.

To verify test strips, the romkey driver 160 reads a code number from aromkey, such as the romkey 40 d, installed in the meter 10. The codenumber typically includes the lot number for the corresponding teststrips and a test type ID stored on the romkey by the manufacturer ofthe meter 10. The test strip 28 has an associated test stripidentification number 172 that is mathematically derived from the codenumber and printed on the test strip itself, the packaging for the teststrip, or a tag packaged with the test strip. The meter 10 prompts theuser to enter the test strip identification number 172 into the meterusing the keypad 46.

The meter 10 also reads the code number from the memory device,mathematically derives a test strip identification number correspondingto the code number, compares the received test strip identificationnumber to the derived test strip identification number, and activatesthe meter for use with the test strip only if the received test stripidentification number corresponds to the derived test stripidentification number. The romkey 40 d also stores an expiration datefor the corresponding test strip 28. The meter 10 reads the expirationdate and activates for use with the test strip 28 and the romkey 40 donly if the expiration date is prior to a current date read by the meterfrom the internal clock 164.

FIGS. 4-14 are logic flow diagrams illustrating examples of thefunctionality that may be implemented by the meter 10 and the system 100for remotely generating health reports. The following description ofthese logic flow diagrams will also refer to the elements shown on FIGS.2 and 3. It should be understood that these examples illustrate the useof these components in producing total cholesterol tests and relatedhealth reports. In particular, the specific diagnostic informationgathered and the specific diagnostic results described are thoseassociated with the well-known Framingham Medical Study, which isincorporated herein by reference. Although this particular programmodule illustrates the operation of an illustrative embodiment of theinvention, those skilled in the art will understand that the meter 10and the system 100 could be programmed with additional and differentprogram modules.

In addition, as the meter 10 is configured with multiple romkey socketsand programmed to accept additional program modules in the future, itwill be appreciated that similar functionality may be implemented in thefuture for blood glucose tests and diabetes-related health reports, AIDStests and related health reports, cancer tests and related healthreports, and so forth. Additional functionality of the meter 10 for usewith a debit-card type payment system is described with reference toFIGS. 30-31.

Meter Activation

FIG. 4 is a logic flow diagram illustrating a routine 400 for activatingthe meter 10. This routine requires that a user enter a properactivation code to activate the meter 10. This typically requires thatthe user call the manufacturer, which provides an opportunity to verifythe meter's authenticity, set up a data file for the meter in the healthreport server, and tell the user how to update the meter software, ifnecessary. If a software update is indicated, the user may be instructedto activate the meter, initialize a smartcard, load the smartcard into acomputer station, and establish a network connection with the healthreport server. The server can then download the new software (e.g., newversion of an existing software module or a new software module) to thesmartcard 54, which, in turn, can be placed back in the meter 10. Thenew software can then be uploaded to the meter.

In step 402, the meter 10 is programmed at the factory by setting theinternal clock 164 to the correct date and storing an activation codealgorithm within the meter. Step 402 is followed by routine 404, inwhich the activation site, typically the manufacturer, computes anactivation code for the current day. That is, each day the activationsite computes a new activation code that is valid only for that day. Theactivation code is computed using the same algorithm that was stored inthe meter 10 in step 402. This algorithm is described below withreference to FIG. 5.

Step 404 is followed by routine 406, in which the activation sitereceives an activation communication for the purpose of activating ameter 10. The user of the meter typically places this communication byplacing a telephone call to a telephone number (e.g., a “1-800” or othertoll-free telephone number) on the meter or on the packaging ordocumentation provided with the meter. Step 406 is followed by routine408, in which the activation site delivers the activation code for thecurrent date to the calling user. Step 408 is followed by routine 410,in which the calling user enters the activation code into the meter 10by manipulating the user input device 36.

Step 410 is followed by step 412, in which the meter 10 verifies thereceived activation code by computing an activation code using itson-board activation code algorithm and the current date read from itsinternal clock 164. In doing so, the meter 10 uses the same algorithmthat was used by the activation site to compute the activation code thatwas delivered to the user and entered into the meter (i.e., thealgorithm described with reference to FIG. 5). Step 412 is followed byroutine 414, in which the meter 10 compares the received activation codeto the computed activation code. Step 414 is followed by routine 416, inwhich the meter 10 determines whether the activation is verified bydetermining whether the received activation corresponds to the computedactivation code.

If the activation is not verified, the “NO” branch is followed from step416 to step 418, in which the meter 10 determines whether a timeoutcondition or an allowed number of tries has been reached. If a timeoutcondition or an allowed number of tries has not been reached, the “NO”branch loops from step 418 to step 410, and the meter 10 displays anerror and prompts the user to reenter the activation code. If a timeoutcondition or an allowed number of tries has been reached, the “YES”branch is followed from step 418 to the “END” step, and the meter 10 isnot activated.

Referring again to step 416, if the activation is verified, the “YES”branch is followed from step 416 to step 420, in which the meter 10 isactivated. Step 412 is followed by the “END” step, in this case with themeter 10 activated.

FIG. 5 is a logic flow diagram illustrating a routine 404 for computingan activation code for the meter 10 or the activation site, referred tocollectively below as the “computing entity.” Routine 404 beginsfollowing step 402 shown on FIG. 4. In step 502, the computing entitygets the day, month, and year (six digit decimal) from the internalclock 164. Step 502 is followed by step 504, in which the computingentity combines the six digits defining the date into a hex value (sixdigit hex). Step 504 is followed by step 506, in which the computingentity applies a predetermined mathematical operation to this hex valueto compute a new hex value (new six digit hex).

Step 506 is followed by step 508, in which the computing entity appliesa mask to the new six digit hex value to obtain a four digit hex value(new four digit hex). In other words, the computing entity selects apredetermined four of the six digits for further processing. Step 508 isfollowed by step 510, in which the computing entity converts this newfour digit hex value to a decimal value (four digit decimal value). Step510 is followed by step 512, in which the computing entity relocates oneor more of the digits and adds one or more null numbers at predefinedlocations (new four digit decimal value). Step 512 is followed by step514, in which the computing entity uses the resulting new four digitdecimal number as the activation code. Step 514 is followed by the“RETURN” step, which goes to step 406 on FIG. 4.

The mathematical operation applied in step 506 may be any of a varietyof algorithms designed to quasi-randomize the result. For example, thedigits may be grouped into subsets that, in turn, are used in one ormore linear mathematical operations, such as addition, subtraction,multiplication, division, raising to a power, raising to a fraction, andthe like. For example, a polynomial formula may be applied to the digitsor subsets of the digits. The digit shuffling operation applied in step512 is also applied to quasi-randomize the result. Many other types ofquasi-randomizing methodologies will be apparent to those skilled in theart.

Test Strip Validation

FIG. 6 is a logic flow diagram illustrating a routine 600 for verifyinga test strip for the meter 10. In step 602, the meter 10 is programmedat the factory with a test strip validation algorithm. Step 602 isfollowed by step 604, in which a romkey with a corresponding lot of teststrips is programmed with a test type ID. This test type ID, togetherwith a lot number for the test strips placed on the romkey by the teststrip manufacturer, forms a four-digit code number that is resident onthe romkey when it leaves the factory.

Step 604 is followed by routine 606, in which a test strip ID ismathematically derived from the romkey code number. Routine 606 isdescribed below with reference to FIG. 7. Routine 606 is followed bystep 608, in which the test strip ID is printed on the lot of teststrips corresponding to the romkey, on the packaging for the teststrips, or tags that are packaged with the test strips. The test stripsare then packaged with corresponding romkeys and distributed for usewith various meters. It should be understood that many identical romkeysmay be produced for each lot of test strips because one romkey isincluded in each distribution-sized package, and a production-sized lotof test strips may be many times larger than a distribution-sizedpackage.

Step 608 is followed by step 610, in which the user of a meter 10 puts aromkey into the meter and enters the corresponding test strip ID intothe meter using the user input device 36. This is the test strip ID thatwas printed on the test strip, its packaging, or a tag packaged with thetest strip in step 608. Step 610 is followed by step 612, in which themeter 10 gets the current date from the internal clock 164, reads thecode number and expiration date from the romkey, and computes a teststrip ID number based on the code number. The test strip ID number isderived from the code number using the same algorithm that was used tocompute the test strip ID number at the factory in routine 606.

Step 612 is followed by step 614, in which the meter 10 determineswhether the current date is prior to the expiration date read from theromkey. If the current date is not prior to the expiration date readfrom the romkey, the “NO” branch is followed to the “END” step, and themeter is not activated for use with the instant romkey. If the currentdate is prior to the expiration date read from the romkey, the “YES”branch is followed to step 616, in which the meter 10 compares thereceived test strip (input by the user) to the computed test strip ID(derived from the code number read from the romkey). Step 616 isfollowed by step 618, in which the meter 10 verifies the test strip ifthe received test strip corresponds to the computed test strip ID.

If the meter 10 verifies the test strip, the “YES” branch is followedfrom step 618 to step 622, in which the meter 10 activates for use withthe instant test strip and romkey. Step 622 is followed by the “END”step. If the meter 10 does not verify the test strip, the “NO” branch isfollowed from step 618 to step 620, in which the meter 10 determineswhether a timeout condition or an allowed number of tries has beenreached. If a timeout condition or an allowed number of tries has notbeen reached, the “NO” branch loops from step 620 to step 610, and themeter 10 displays an error and prompts the user to reenter the teststrip ID and/or insert the correct romkey. If a timeout condition or anallowed number of tries has been reached, the “YES” branch is followedfrom step 620 to the “END” step, and the meter 10 is not activated forthe instant test strip and romkey.

Test Strip ID Assignment

FIG. 7 is a logic flow diagram illustrating routine 606 for computing atest strip ID for the meter 10. Routine 606 begins following step 604shown on FIG. 6. In step 702, the meter 10 reads the code number (i.e.,lot number plus test type ID) from the romkey. Step 702 is followed bystep 704, in which the meter 10 converts this four digit decimal valueto 16-bit binary value. Step 704 is followed by step 706, in which themeter 10 applies a predetermined mathematical operation to this 16-bitbinary value.

Step 706 is followed by step 708, in which the meter 10 checks a valueat a predetermined bit of the 16-bit binary value. Step 708 is followedby step 710, in which the meter 10 performs a conditional bit swap. Thatis, a first type of bit swap is performed if the value of the checkedbit is a “1” and a second type of bit swap is performed if the value ofthe checked bit is a “0.” Step 710 is followed by step 712, in which themeter 10 converts the resulting number to a four digit decimal value.Step 712 is followed by step 714, in which the meter 10 uses theresulting four digit decimal number as the test strip ID. Step 714 isfollowed by the “RETURN” step, which goes to step 608 on FIG. 6.

The mathematical operation applied in step 706 may be any of a varietyof algorithms designed to quasi-randomize the result. For example, thedigits may be grouped into subsets that, in turn, are used in one ormore linear mathematical operations, such as addition, subtraction,multiplication, division, raising to a power, raising to a fraction, andthe like. For example, a polynomial formula may be applied to the digitsor subsets of the digits. The digit shuffling operation applied in steps708 and 710 is also applied to quasi-randomize the result. Many othertypes of quasi-randomizing methodologies will be apparent to thoseskilled in the art.

Diagnostic Data Entry

FIG. 8 is a logic flow diagram illustrating a routine 800 for enteringdiagnostic program modules into the meter 10. In step 802, the meter 10is programmed at the factory with one or more initial diagnosticalgorithms. In addition, a computer maintained at the programming site,typically the manufacturer, is programmed with a cross reference tableindicating the serial number for the meter and the version number ofeach diagnostic program module installed in the meter 10.

At some later point, a user downloads medical data from the meter 10 toa smartcard in the course of normal meter use. At this time, the serialnumber for the meter is also stored on the smartcard. The smartcard isthen read by a computer station, which establishes a network connectionwith a programming server, which may be the same as, or coordinatedwith, the health report server 102 shown on FIG. 2. At step 804, theprogramming server receives the data that was stored on the smartcard.Step 804 is followed by step 806, in which the programming serverinstructs the computer station to erase the unsecured data stored on thesmartcard. That is, the computer station erases the medical data storedin the unsecure memory but does not erase the PIN or any data stored inthe secure memory.

Step 806 is followed by step 808, in which the programming server getsthe serial number for the meter 10 from the received data and looks upthe version numbers for the diagnostic program modules installed on themeter. Step 808 is followed by step 810, in which the programming serverdetermines whether the meter 10 includes the latest version of all ofthe program modules that should be installed on the meter. If the meter10 includes the latest version of all of the program modules that shouldbe installed on the meter, the “YES” branch is followed to the “END”step, and the meter software is not updated.

If, on the other hand, the meter 10 does not include the latest versionof all of the program modules that should be installed on the meter, the“NO” branch is followed to step 812, in which the programming serverloads new diagnostic program modules, new versions of diagnostic programmodules, or updates for existing program modules on the smartcard. Atsome later point in step 814, the to smartcard is placed back in themeter 10. At this point, step 814 is followed by step 816, in which thenew diagnostic program modules, new versions of diagnostic programmodules, or updates for existing program modules stored on the smartcardare uploaded to the meter 10. Step 816 is followed by the “END” step.

Diagnostic Analysis

FIG. 9 is a logic flow diagram illustrating a routine 900 for computingimmediate diagnostic results in the meter 10, and for remotely producinghealth reports. In step 902, the meter 10 prompts the user to select aromkey and insert a corresponding test strip, with a blood sample, intothe meter. Step 902 is followed by step 904, in which the meter 10prompts the user to select a desired diagnostic program modulecorresponding to the type of test strip inserted into the meter. Step904 is followed by step 906, in which the meter 10 performs the teststrip verification algorithm shown on FIG. 6 and, if the test strip isverified, obtains test results.

Step 906 is followed by routine 908, in which the meter 10 prompts theuser for additional diagnostic information. Routine 908 is describedbelow with reference to FIG. 10. Routine 908 is followed by routine 910,in which the meter 10 computes immediate diagnostic results. Routine 910is described below with reference to FIG. 11. Routine 910 is followed bystep 912, in which the meter 10 displays the diagnostic results on thedisplay device 34. Step 912 is followed by step 914, in which the meter10 stores the test results, the diagnostic information, and thediagnostic results (and also stores the meter's serial number) on thesmartcard.

At some later point, in step 916 the user reads the smartcard with acomputer station. Step 916 is followed by step 918, in which thecomputer station establishes a network connection with the health reportserver 102. Step 918 is followed by step 920, in which the computerstation downloads the data from the smartcard to the health reportserver 102. Step 920 is followed by routine 922, in which health reportserver 102 receives additional diagnostic and health report informationfrom the user of the computer station and compiles a personal healthreport based on the data received from the computer station. Routine 922is described below with reference to FIG. 12. Routine 922 is followed bystep 924, in which the health report server 102 transmits the healthreport to the computer station, where the health report is printed anddelivered to the patient. Step 924 is followed by the “END” step.

FIG. 10 is a logic flow diagram illustrating routine 908 for obtainingcholesterol-related diagnostic information for the meter 10. Routine 908begins following step 906 shown on FIG. 9. In step 1002, the meter 10prompts for and receives the patient's gender. Step 1002 is followed bystep 1004, in which the meter 10 prompts for and receives the patient'sethnicity. Step 1004 is followed by step 1006, in which the meter 10prompts for and receives an indication of the patient's family historyof heart disease. Step 1006 is followed by step 1008, in which the meter10 prompts for and receives an indication of the patient's personalhistory of heart disease.

Step 1008 is followed by step 1010, in which the meter 10 prompts forand receives an indication of whether the patient is a type-1 diabetic.Step 1010 is followed by step 1012, in which the meter 10 prompts forand receives an indication of whether the patient is a type-2 diabetic.Step 1012 is followed by step 1014, in which the meter 10 prompts forand receives an indication of whether the patient is a smoker.

Step 1014 is followed by step 1016, in which the meter 10 prompts forand receives an indication of the patient's height. Step 1016 isfollowed by step 1018, in which the meter 10 prompts for and receives anindication of the patient's weight. Step 1018 is followed by step 1020,in which the meter 10 prompts for and receives an indication of thepatient's age. Step 1020 is followed by step 1022, in which the meter 10prompts for and receives an indication of the patient's blood pressure.Step 1022 is followed by step 1024, in which the meter 10 prompts forand receives an indication of the patient's fitness. Step 1024 isfollowed by the “RETURN” step, which goes to routine 910 shown on FIG.9. It will be appreciated that the preceding list of diagnosticinformation is only illustrative of the type of information that may begathered, and that less data, different data, or more data could begathered, if desired.

FIG. 11 is a logic flow diagram illustrating routine 910 for computingimmediate cholesterol-related diagnostic results for the meter 10.Routine 910 begins following routine 908 shown on FIG. 9. In step 1102,the meter 10 prompts for and receives a selection of a diagnosticalgorithm resident on the meter. Step 1102 is followed by step 1104, inwhich the meter 10 gets total cholesterol test results from the testinstrument module 158 or, if they are not available, prompts the user toinput the test results manually.

Step 1104 is followed by step 1106, in which the meter 10 calculates anddisplays a medical risk index associated with heart disease or heartattack, such as “very high,” “high,” “moderate,” “low,” or “very low.”Step 1106 is followed by step 1108, in which the meter 10 calculates anddisplays a recommended weight loss, if appropriate. Step 1108 isfollowed by step 1110, in which the meter 10 calculates and displays a5-year cardiac risk (e.g., risk of cardiac arrest in five years is 10%).Step 1110 is followed by step 1112, in which the meter 10 calculates anddisplays a 10-year cardiac risk (e.g., risk of cardiac arrest in tenyears is 20%).

Step 1112 is followed by step 1114, in which the meter 10 calculates anddisplays a cardiac age (to compare against the patient's chronologicalage). Step 1112 is followed by step 1114, in which the meter 10calculates and displays an extended cardiac age (e.g., cardiac agecompared to chronological age for five, ten, fifteen, etc. years intothe future). Step 1116 is followed by step 1118, in which the meter 10calculates and displays a medical risk index associated with stroke,such as “very high,” “high,” “moderate,” “low,” or “very low.” Step 1118is followed by the “RETURN” step, which goes to step 912 on FIG. 9. Itwill be appreciated that the preceding list of diagnostic results isonly illustrative of the type of information that may be generated, andthat less data, different data, or more data could be generated, ifdesired.

Remote Health Report Generation

FIG. 12 is a logic flow diagram illustrating routine 922 for remotelyproducing health reports. Routine 922 begins following step 920 shown onFIG. 9. In step 1202, in which the health report server 102 prompts forand receives a new drug therapy, such as a cholesterol-loweringprescription. Step 1202 is followed by step 1204, in which the healthreport server 102 gets a prescription data sheet for the drug therapy.This data sheet typically includes instructions for taking theprescription, such as dosage, times to take each dose, whether to takewith food or liquid, whether to avoid driving, pregnancy-relatedinstructions, foods to avoid, and so forth.

Step 1204 is followed by step 1206, in which the health report server102 prompts for and receives information regarding any otherprescription drugs that the patient is currently taking. Step 1206 isfollowed by step 1208, in which the health report server 102 getscross-reaction information regarding the new drug therapy and the othercurrent drug prescriptions. Step 1208 is followed by step 1210, in whichthe health report server 102 prompts for and receives a specificdescription of exercise therapy for the patient, or a selection ofstandard exercise sections for inclusion in the health report. Step 1210is followed by step 1212, in which the health report server 102 promptsfor and receives diet therapy for the patient, or a selection of astandard diet section for inclusion in the health report. Step 1212 isfollowed by step 1214, in which the health report server 102 prompts forand receives indications of additional standard sections for inclusionin the health report.

Step 1214 is followed by step 1216, in which the health report server102 assembles the preceding information for inclusion in a healthreport. Step 1216 is followed by step 1218, in which the health reportserver 102 prompts for and receives trend analysis selections. Step 1218is followed by step 1220, in which the health report server 102 preparesthe selected trend analysis, such as total cholesterol and blood glucoselevels over a series of tests. The trend analysis may be provided aloneor as part of the health report. Step 1220 is followed by step 1222, inwhich the health report server 102 assembles the preceding informationinto a health report and/or trend analysis report. Step 1222 is followedby the “RETURN” step, which goes to step 924 shown on FIG. 9. It will beappreciated that the preceding list of health report information is onlyillustrative of the type of information that may be compiled, and thatless data, different data, or more data could be compiled, if desired.

Smartcard PIN Security

FIG. 13 is a logic flow diagram illustrating a routine 1300 for savingmedical data to the PIN-secured removable memory storage device 54,represented by a smartcard. In step 1302, a user places the smartcard inthe meter 10. Step 1302 is followed by step 1304, in which the meter 10prompts for and receives a PIN from the user. Step 1304 is followed bystep 1306, in which the meter 10 reads the PIN field on the smartcard.Step 1306 is followed by step 1308, in which the meter 10 determineswhether the PIN field is occupied (i.e., whether a PIN has beenpreviously stored on the smartcard).

If the PIN field is not occupied, the “NO” branch is followed from step1308 to step 1310, in which the meter 10 stores the PIN received fromthe user in the PIN field on the smartcard. Step 1310 is followed bystep 1314, in which the meter 10 activates for use with the currentsmartcard. Step 1314 is followed by the “END” step.

Referring again to step 1308, if the PIN field is occupied, the “YES”branch is followed to step 1312, in which the meter 10 determineswhether the PIN received from the user matches the PIN stored in the PINfield on the smartcard. If the PIN received from the user matches thePIN stored in the PIN field on the smartcard, the “YES” branch isfollowed to step 1314, in which the meter 10 activates for use with thecurrent smartcard. Step 1314 is followed by the “END” step.

Referring again to step 1312, if the PIN received from the user does notmatch the PIN stored in the PIN field on the smartcard, the “NO” branchis followed to step 1314, in which the meter 10 determines whether atimeout condition or an allowed number of tries has been reached. If atimeout condition or an allowed number of tries has not been reached,the “NO” branch is followed to step 1318, in which the meter 10 displaysan error and prompts the user to reenter the activation code. From step1318, routine 1300 loops to step 1312. If a timeout condition or anallowed number of tries has been reached, the “YES” branch is followedfrom step 1316 to the “END” step, and the meter 10 is not activated foruse with the instant smartcard.

Secure Medical Records Maintenance System

FIG. 14 is a functional block diagram of a system for using the meter 10in connection with a secure medical records maintenance system 1400. Themeter 10 stores a patient's test results and diagnostic information on aremovable memory storage device, such as the smartcard 54. Aconventional interface 106 may then be used to interface the smartcard54 with a conventional desktop, laptop or other type of computer 108,which in turn communicates with other computers over a network-basedcomputer system, such as the Internet 110. As discussed previously, thisInternet link may be used to produce a printed health report booklet 112including a health assessment based on a patient's test results anddiagnostic information, which a health-care provider typically providesto the patient.

Although this secure medical records maintenance system 1400 isspecifically adapted for use with the meter 10, it may be used to storeany type of electronic medical records, and is particularly convenientfor storing a wide range of electronic medical data generated remotelyfrom the hospital or doctor's office environment. In addition, thesecure medical records maintenance system 1400 may read medical datastored on memory storage devices other than the smartcard 54, and mayoperate over computer networks other than the Internet 100.

The secure medical records maintenance system 1400, which is presentlyknown as the “PRIVALINK” system, operates in connection with a softwaremodule 1402 installed on the accessing computer 108. This software ispresently known as the “PRIVALINK” user site software. The server-side“PRIVALINK” system 1400 includes a first remote server 1404 that storespatient identification information, a second remote server 1406 thatstores patient medical data, an encryption/decryption module 1408 thatimplements encryption and other security-related functions, and abooklet generation module 1410, which produces printed health reportbooklets 112 based on the information stored in the servers 1404, 1406.The patient identification information and medical data are maintainedin separate, secure servers 1404, 1406 to prevent correlation of aspecific patient's medical data with the associated patientidentification information.

Because the data on the servers 1404, 1406 is separate and secure fromeach other, access may be granted to either server without identifyingany particular patient's medical data. For example, access may begranted to the first remote server 1404, but not to the second server1406, for the purpose of generating a mailing list of patients withoutdivulging any medical data associated with the patients. Similarly,access may be granted to the second remote server 1406, but not to thefirst server 1404, for the purpose of conducting investigative analysesinvolving patient medical data without divulging any patientidentification information associated with the medical data.

For further data security and because each smartcard 54 only has alimited data storage capability, the medical data stored on eachsmartcard may be automatically erased from the smartcard after the datais entered into the second remote server 1406. To obtain the medicaldata, the smartcard 54 is received within the meter 10, which stores themedical data on the smartcard. And to download the medical data to themedical records maintenance system 1400, the removable memory storagedevice is receivable within the interface 106 for communication with thecomputer 108, which is operable for transmitting the medical data to thesecond remote server 1406 over the Internet 110.

FIG. 15 is software architecture diagram illustrating a system forconducting secure communications between the computer 108 and the securemedical records maintenance system 1400. The “PRIVALINK” user sitesoftware 1402 includes an encryption/decryption module 1412 thatimplements encryption/decryption services on the client computer 108. Acorresponding encryption/decryption module 1408 on the secure medicalrecords maintenance system 1400 implements complimentaryencryption/decryption services on the server side, typically using awell-known encryption/decryption package, such as that known as“BLOWFISH” or “DES.” The server-side encryption/decryption module 1408also maintains access to a table of valid professional registrationnumbers 1411, typically DEA numbers, received from the registeringagency. This table is used to validate the professional registrationnumbers of practitioners attempting to access the secure medical recordsmaintenance system 1400.

The server-side encryption/decryption module 1408 also maintains arecord of all transactions with accessing computers for future analysis.In addition, all data transfers from the secure medical recordsmaintenance system 1400 to the user site 108, such as health reportbooklets 112, are encrypted/decrypted through an Internet secure socketslayer connection 1500, which is well known to those skilled in the art.These encryption/decryption services prevent theft or inadvertent lossof patient medical data through unintended transmission or extraction ofcommunications occurring on the Internet 110.

The “PRIVALINK” user site software 1402 also implements clientapplication, certification and login processes for accessing the securemedical records maintenance system 1400. The application, certificationand login process is described below with reference to FIGS. 17-19. Uponsuccessful login to the secure medical records maintenance system 1400,the “PRIVALINK” user site software 1402 implements a menu-driven userinterface system 1414 for conducting communications between thepractitioner computer 108 and the secure medical records maintenancesystem 1400. This interface system includes a health care provider dataentry screen 2100 shown in FIG. 21, a patient address data entry screen2500 shown in FIG. 25, a patient test data entry screen 2600 shown inFIG. 26, a booklet selection screen 2700 shown in FIG. 27, and a bookletpreview/printing screen 2800. The menu-driven user interface system 1412also includes other related user interface screens. The operation of themenu-driven user interface system 1412 is described below with referenceto FIG. 17.

FIG. 16 a functional block diagram illustrating security aspects of thesecure medical records maintenance system 1400. The secure medicalrecords maintenance system 1400 preferably includes a large number ofsmartcards 54 a-n, which operate in concert with a large number ofmeters 10 a-n. Although each smartcard 54 a-n is preferably used tostore medical data for an associated patient, each card could be used tostore medical data for multiple patients. Each smartcard 54 also storesa patient-specified personal identification number (PIN), and may storePINs for multiple patients if the smartcard is configured to storemedical data for multiple patients. Each PIN is used to gain access to asecure storage area on the smartcard 54, which stores an associatedpatient identification number and medical records identification number,which are assigned by the secure medical records maintenance system1400.

The first remote server 1404 of the secure medical records maintenancesystem 1400 stores patient identification information indexed by patientidentification numbers, and the second remote server 1406 stores patientmedical data indexed by the medical records identification numbers.Typically, each patient identification number and medical identificationnumber is a unique number assigned by the operator of the secure medicalrecords maintenance system 1400 upon entry of each patient into thesystem. For example, the patient identification numbers and medicalidentification numbers may be social security numbers or sequentialregistration numbers. Alternatively, the patient identification numbersand medical identification numbers may be unique numbers computed by anon-repeating pseudo-random number generator. The patient identificationnumber and the medical records identification number may be 16-bithexadecimal or another suitable value. In addition, either or both ofthe patient identification number and the medical records identificationnumber may be a global user identification number (GUID), which is asecure communication key generated by well-known secure encryptionsystems, such as currently available private-key and public-keyencryption systems including “BLOWFISH,” “DES” and others. Many otherschemes for assigning unique patient identification numbers will becomeevident to those skilled in the art.

For security purposes, the medical data maintained in the second remoteserver 1406 cannot be correlated to the associated patientidentification information maintained in the first remote server 1408based on the information contained in the first and second remoteservers. To allow correlation of the data stored in the two servers1404, 1406 the secure medical records maintenance system 1400 includes acorrelation table 1600 uniquely associating each medical recordsidentification number with a particular one of the patientidentification numbers. The correlation table 1600 for a particularpatient typically resides in the PIN-secured storage area on thepatient's smartcard 54. The correlation table 1600 for a practitioner'spatients may also reside on the practitioner's computer 108, such as adoctor's or pharmacist's computer, that is associated with a licensedmedical practitioner having an assigned professional registration number(DEA number). Each practitioner's correlation table 1600 is preferablyencrypted and maintained in a secure file. The proprietor of the securemedical records maintenance system 1400 may also maintain a completeback-up correlation table 1600, typically in a secure encrypted filelocated on a separate file server.

For further security, the first and second remote servers 1404, 1406 areaccessed by the practitioners' computers 108 a-n through encryptedcommunications secured by an application procedure that includesvalidation of the practitioner's registration number (DEA number). Thisaccess will be limited to medical records and patient identificationinformation associated with the accessing practitioner. In other words,each practitioner will only have access to his or her patients' medicalrecords and patient identification information.

Similar access procedure may be implemented for individual patients,except that access will be limited to that particular patient's medicalrecords and patient identification information. For example, individualpatients may register in advance with the proprietor of the system 1400,which will issue each patient a unique registration number. In thiscase, the first and second remote servers 1404, 1406 may accessed bycomputers operated by the individual patients through encryptedcommunications secured by an application procedure that includesvalidation of the patient's registration number.

For both practitioners and individual patients, the applicationprocedure may be further secured by receipt and validation of aclient-supplied PIN. Moreover, the application procedure typicallyincludes issuance of a client certificate insuring that access to thefirst and second remote servers occurs from the client computer thatinitiated the application and certification process.

Those skilled in the art will appreciate that the data distributionsystem implemented by the secure medical records maintenance system 1400includes many aspects of data security. For example, a patient's medicalrecords identification number cannot be obtained from the patient'ssmartcard 54 without access to the patient-assigned PIN. In addition,while the patient's medical data is indexed by the patient's medicalrecords identification number in the second server 1406, the patient'sname and other identification information cannot be retrieved from thefirst server 1404 using this data. Similarly, a hacker obtaining assessto one or both of the servers 1404, 1406 cannot correlate patientidentification information with patient medical data. In addition, thecorrelation data for the entire secure medical records maintenancesystem 1400 is distributed among the various smartcards 54 a-n andpractitioner computers 108 a-n registered for use with the system. Thus,a hacker cannot obtain the correlation data for any single patient, muchless the entire database, through access to the centrally-maintaineddata servers 1404, 1406.

For further security, the secure medical records maintenance system 1400cannot be accessed from the a medical practitioner's computer 108without knowledge of the proper practitioner-assigned PIN. And allcommunication between the practitioner's computer 108 and the securemedical records maintenance system 1400 are encrypted for transmissionsecurity. Furthermore, each correlation table 1600, which provides thelink between patient identification numbers and medical recordsidentification numbers for a particular practitioner, may itself beencrypted, with the key to this encryption stored in a separatelocation. For example, this encryption key may be a practitioner PIN orGUID stored on a PIN-secured area the practitioner's computer 108 or ona smartcard 54 assigned to the practitioner.

FIG. 17 is a logic flow diagram illustrating an illustrative process1700 for communicating with the secure medical records maintenancesystem 1400. In routine 1702, a medical practitioner conducts a clientapplication procedure to obtain a secure client certificate, which isalso known as a “CA” or certificate-authentication. Routine 1702 isdescribed in greater detail with reference to FIG. 18. Routine 1702 isfollowed by a client login procedure 1704, which is described in greaterdetail with reference to FIG. 19. These procedures ensure that access tothe secure medical records maintenance system 1400 is limited toregistered medical practitioners using the same computer and browserthat the practitioner used to obtain a secure client certificate throughthe application procedure. That is, any attempt to access the securemedical records maintenance system 1400 by a person without a valid DEAnumber, or from a non-certified computer or browser, will be rejected.As noted previously, similar procedures may be implemented for allowingindividual patients to access their records on the secure medicalrecords maintenance system 1400.

FIG. 18 is a logic flow diagram illustrating routine 1702 used by amedical practitioner to apply for access to the secure medical recordsmaintenance system 1400. Routine 1702 begins at the start of FIG. 17. Instep 1802, the client-side PRIVALINK software 1402 issues a clientapplication request to the server-side encryption/decryption module1408, which initiates a transaction document record for thecommunication. That is, all communications between the client-sidePRIVALINK software 1402 and the server-side encryption/decryption module1408 are recorded for future analysis by the server-sideencryption/decryption module 1408. The client application request istypically received by an Internet link to a specified web pageassociated with the server-side encryption/decryption module 1408. Themedical practitioner can obtain the proper Internet address by placing atelephone call to the operator of the system 1400. The phone number, andpossibly the Internet address, will be printed on each meter 10 and mayalso be available through other forms of notification, such asadvertisement and direct-mail notification to licensed practitioners(e.g., physicians and pharmacists).

Step 1802 is followed by step 1804, in which the PRIVALINK software 1402displays an application screen and receives client input including thepractitioner's professional registration number, typically a DEA number.Step 1804 is followed by step 1806, in which the PRIVALINK software 1402receives a certification request including selection of an encryptiontype. This is typically associated with completion of the data-entryfields of the application screen and selection of a “submit” controlitem. Step 1806 is followed by step 1808, in which the PRIVALINKsoftware 1402 downloads an encryption program module from theserver-side encryption/decryption module 1408, such as an “ACTIVE X”control or applet, to the client's computer 108. This encryption programmodule typically includes a “key” or nugget of information to be storedin the accessing browser. The server-side encryption/decryption module1408 can later check an accessing computer for the presence of the “key”to ensure that the accessing computer and browser is the same as the onegoing through the application procedure.

Step 1808 is followed by step 1810, in which the server-sideencryption/decryption module 1408 validates the registration number(e.g., DEA number) entered by the applicant, typically by comparing thereceived registration number to the table of valid registration numbers1411 received from the registration authority (e.g., table of valid DEAnumbers). If the registration number is properly validated, step 1810 isfollowed by step 1812, in which the server-side encryption/decryptionmodule 1408 transmits an e-mail message to the PRIVALINK software 1402including a URL for accessing the secure servers 1404, 1406. Step 1812is followed by step 1814, in which the PRIVALINK software 1402 transmitsa client link to the designated URL. Upon receipt of the link, theserver-side encryption/decryption module 1408 checks for the presence ofthe “key” to ensure that the accessing computer and browser is the sameas the one that went through the application procedure.

If the “key” is properly validated, step 1814 is followed by step 1816,in which the server-side encryption/decryption module 1408 transmits a“server root CA” and a “client certificate” to the PRIVALINK software1402 on the client's computer 108. Step 1816 is followed by step 1818,in which the PRIVALINK software 1402 links the applicant to a securearea of the encryption/decryption module 1408, which validates thepresence of the server root CA. If the server root CA is properlyvalidated, step 1818 is followed by step 1820, in which the PRIVALINKsoftware 1402 prompts the user to identify the client certificate foruse in the transaction. If the client certificate is properly validated,step 1820 is followed by step 1822, in which the PRIVALINK software 1402links the applicant to a login screen. Step 1822 is followed by step1824, in which the encryption/decryption module 1408 saves thetransaction documentation for the client's application procedure. Step1824 is followed by the “CONTINUE” step, which returns to routine 1704shown in FIG. 7.

FIG. 19 is a logic flow diagram illustrating a routine 1704 for logginginto the secure medical records maintenance system 1400. Routine 1704begins following routine 1702 shown in FIG. 7. In step 1902, thePRIVALINK software 1402 displays a login screen on the client's computer108. Step 1902 is followed by step 1904, in which the PRIVALINK software1402 loads the client's registration number, which was obtained duringthe application procedure described with reference to FIG. 18, into thelogin screen. That is, an accessing client does not have an opportunityto enter the login procedure without having first having gone throughthe application procedure described with reference to FIG. 18, whichrequires the applicant to provide a valid registration number, whichtypically may be a DEA number for a licensed medical practitioner or aregistration number issued by the proprietor of the secure medicalrecords maintenance system 1400 for an individual patient.

Step 1904 is followed by step 1906, in which the PRIVALINK software 1402receives the practitioner's personal identification number (PIN). Step1906 is followed by step 1908, in which the encryption/decryption module1408 validates the practitioner's personal identification number (PIN)for use with the received professional registration number. Step 1908 isfollowed by step 1910, in which the encryption/decryption module 1408determines whether the received PIN is a new PIN for use in connectionwith the received professional registration number. If the received PINis a new PIN for use in connection with the received professionalregistration number, the “YES” branch is followed from step 1910 to step1912, in which the PRIVALINK software 1402 prompts the user to completethe interface screens 2000-2007 (FIGS. 20-27). Step 1912 and the “NO”branch from step 1910 are followed by step 1914, in which the client islinked to the interface screens 2000-2007 (FIGS. 20-27). Step 1914 isfollowed by “CONTINUE” step, which returns to step 1706 shown on FIG. 7.

User Interface Design

Referring again to FIG. 17, once the medical practitioner hassuccessfully logged into the secure medical records maintenance system1400, routine 1704 is followed by step 1706, in which the PRIVALINKsoftware 1402 displays a “switchboard” user interface 2000. FIG. 20 isan illustration of a typical “switchboard” user interface 2000, whichincludes a number of selection items corresponding to functionsavailable on the server. For example, the interface 2000 typicallyincludes a “provider” selection item 2002 and a “patients” selectionitem 2004. To illustrate the operation of the user interface it isassumed that the practitioner initially selects the “provider” selectionitem 2002. Thus, step 1706 is followed by step 1708, in which thePRIVALINK software 1402 receives a “provider” selection from the“switchboard” user interface 2000.

Step 1708 is followed by step 1710, in which the PRIVALINK software 1402displays an “address” user interface 2100. FIG. 21 is an illustration ofa typical “address” user interface 2100. The interface 2100 includes afirst field 2102 for entering a practitioner registration number,typically a DEA number, and a second field 2104 for entering apractitioner-assigned PIN. The interface 2100 also includes a number ofother fields for entering the practitioner's contact information, suchas address, phone number, and so forth. The interface 2100 also includesan “address” tab 2106, a “billing info” tab 2108, and a “cover letter”tab 2110 displayed adjacent to the user interface 2100. These tabs allowthe user to toggle among corresponding user interface screens. As notedabove, the interface 2100 initially appears in a “default” mode with the“address” tab 2106 selected.

For example, step 1710 may be followed by step 1712, in which thePRIVALINK software 1402 displays a “billing info” user interface inresponse to user selection of the “billing info” tab 2108. FIG. 22 is anillustration of a typical “billing information” user interface 2108. Theinterface 2100 includes a number of fields 2202 for entering paymentauthorization, such as a bank credit or debit card number. The interface2100 may include other types of payment options, such as a bank accountnumber for wire transfers, authorization to include the charges on atelephone bill or Internet service provider bill associated with theInternet link to the server-based system 1400, reference to anauthorized account for billing at a later date, and the like.

Similarly, step 1712 may be followed by step 1714, in which thePRIVALINK software 1402 displays a “cover letter” user interface 2300 inresponse to user selection of the “cover letter” tab 2110. FIG. 23 is anillustration of a typical “cover letter” user interface 2300. Thisinterface allows the practitioner to author a cover letter that will beincluded with a health report booklet to be produced by the bookletgeneration module 1410 on the server-based system 1400, as describedpreviously with reference to FIG. 9. This allows the practitioner tocustomize the cover letter for each health report booklet produced bythe system.

To further illustrate the operation of the user interface, it is assumedthat the practitioner next selects the “patients” selection item 2004 onthe “switchboard” user interface 2000. Thus, step 1714 is followed bystep 1716, in which the PRIVALINK software 1402 displays a “patients”user interface 2400. FIG. 24 is an illustration of a typical “patientselection” user interface 2400. This user interface allows thepractitioner to select a preexisting patient and to enter new patients.Upon entry of a new patient, the PRIVALINK software 1402 typicallyassigns a unique patient identification number and a unique medicalrecords identification number to the patient, which the user site“PRIVALINK” software 1402 stores in a correlation table 1600, asdescribed previously with reference to FIG. 16.

Step 1716 is followed by step 1718, in which the PRIVALINK software 1402displays a “patient information” user interface 2500. FIG. 25 is anillustration of a typical “patient information” user interface 2500.This interface includes a number of fields for entering patientidentification information, such as address, phone number, and so forth.As described previously with reference to FIG. 16, this patientidentification information is typically indexed by the patientidentification number and stored in the first server 1404, whereas thepatient's medical data is typically indexed by the patient's medicalrecords identification number and stored in the second server 1406.

Step 1718 is followed by step 1720, in which the PRIVALINK software 1402displays a “questionnaire data” user interface 2600. FIG. 26 is anillustration of a typical “questionnaire data” user interface 2600. Thisinterface includes a number of fields for entering patient diagnosticinformation, such as family history, age, weight, body fat, and soforth. This interface may be used to enter patient diagnosticinformation in addition to that received through the meter 10. Forexample, the interface 2600 may be used to enter diagnostic data thatthe meter would have recorded, but the patient failed to enter the datainto the meter 10. In addition, the interface 2600 may be automaticallyfilled in, either partially or completely, with the appropriate datastored on a corresponding smartcard 54. This step may require entry ofan appropriate patient PIN for the corresponding smartcard 54 into theinterface 2600. The interface 2600 may also be used to change orsupplement the data read from the smartcard 54, or enter additionaldiagnostic information that the meter 10 is not configured to collectfrom the patient.

Step 1720 is followed by step 1722, in which the PRIVALINK software 1402displays a “generate reports” user interface 2700. FIG. 27 is anillustration of a typical “generate reports” user interface 2700. Thisinterface includes a number of fields for selecting items to be includedin a patient's health report booklet, such as cover letter, summary,evaluation, and so forth. The interface includes a number of fields forselecting therapy items to be prescribed for the patient and reflectedin the patient's health report booklet, such as lifestyle therapy, lipiddrug prescription, blood pressure drug prescription, and so forth.

FIG. 28 is an illustration of typical health report charts generated bythe secure medical records maintenance system 1400 for inclusion in apatient's health report booklet. These charts include a “coronary riskfactors” chart 2802, a “personal health consequences” chart 2804, and an“extended health assessment” chart 2806. The “coronary risk factors”chart 2802 includes test results and diagnostic information along withideal ranges and patient goals for these items. The “personal healthconsequences” chart 2804 includes interpretive data, such as poundsoverweight, cardiac age, and stroke risk. The “extended healthassessment” chart 2806 includes a projection of future interpretivedata, such as a projected comparison of the patient's chronological ageand cardiac age.

FIG. 29 is an illustration of an additional health assessment chart 2900generated by the secure medical records maintenance system 1400 forinclusion in a patient's health report booklet. This chart includes apictorial representation of cardiac risk factors, such as gender,smoker, personal history, and so forth. The health assessment chart 2900typically presents a pictorial assessment of the “coronary risk factors”shown in chart 2802.

Smartcard Payment System

The system described above is largely dependent on the sale ofproprietary test strips 28 for the collection of revenue from end users.That is, the meter 10 may be made available to individual patients atlittle or no cost, with the sale of proprietary test strips 28 providinga major source of revenue for the proprietor of the health monitoringmeter. This may be a desirable business model for deploying the meters10 because it minimizes the initial cost that an individual patient mustpay to begin using the device. Having to sell each meter 10 at its fullcost, on the other hand, would undermine the economic feasibility ofusing the meter in many contexts.

Nevertheless, it may also be desirable to provide a meter 10 that doesnot rely on the sale of proprietary test strips 28 as a major source ofrevenue. For example, the meter may be adapted to read non-proprietarytest strips, or may incorporate a reusable and/or non-invasive testingdevice, such as an electrode, blood pressure monitoring device, sonictesting device, thermometer, saliva testing device, optical testingdevice, and the like. Of course, a non-invasive multi-use testing devicemay be used many times without affording the proprietor of the healthmonitoring device an opportunity collect revenue associated with use ofthe device.

To solve this problem, the smartcard 54 may be utilized as a type of“debit card” for use with the meter 10. That is, the smartcard 54 devicemay be purchased with a monetary value, or it may have a monetary valuethat is replenishable over the Internet using a bank credit or debitcard or other conventional payment source. The meter 10 may then deductthe cost of performing particular services (e.g., blood cholesteroltest, health assessment, blood sugar test, AIDS test, etc.) from themonetary value represented by the monetary balance stored on thesmartcard 54. In other words, the meter 10 may be configured to activatefor the performance of a variety of services upon deducting a charge forthe selected service from a monetary value stored on a smartcard 54inserted into the device.

FIG. 30 is a logic flow diagram illustrating a routine 3000 for adding amonetary value to a smartcard 54 for use with the meter 10. Althoughsingle-use smartcard could be sold with a monetary value for use withthe meter 10, the cost of the smartcards makes a replenishable debitcard system preferable. In step 3002, the proprietor of the system loadsan illustrative smartcard 54 with debit card software and a zerobalance. Step 3002 is followed by step 3004, in which the smartcard 54is issued for use with the meter 10. For example, the smartcard 54 maybe sold or given away separately or in connection with a meter 10.Typically, the proprietor of the system will be motivated to make boththe meter 10 and the smartcard 54 available for little or no acquisitioncost because the cost of these assets will be recovered through use ofthe debit-card type smartcard 54 with meter 10.

Step 3004 is followed by step 3006, in which the user establishes a PINand activates the smartcard 54, which can be performed using the meter10 or a conventional computer 108 having a smartcard interface 106, asshown in FIG. 2. Step 3006 is followed by step 3008, in which the userloads the smartcard 54 into a conventional computer 108 having asmartcard interface 106 (if the smartcard in not already loaded) andaccesses a predefined debit card Internet site by linking to anassociated URL, which may be printed on the smartcard or made availablethrough advertisement, direct mail, or other communication media. Thedebit card Internet site may typically be a separate server operated bythe proprietor of the secure medical records maintenance system 1400, orit may be another site operated by a separate proprietor. Step 3008 isfollowed by step 3010, in which the debit card Internet site establishescommunications with the smartcard 54 and verifies the authenticity ofthe smartcard.

Step 3010 is followed by step 3012, in which the debit card Internetsite prompts the user for input payment authorization for a monetaryvalue to be added to the smartcard. The debit card Internet site mayaccept a variety of payment options, such as a bank credit or debit cardnumber, a bank account number for wire transfers, authorization toinclude the charges on a telephone bill or Internet service providerbill associated with the Internet link, and the like. Step 3012 isfollowed by step 3014, in which the debit card Internet site validatesthe received payment authorization. Step 3014 is followed by step 3016,in which the debit card Internet site determines whether the receivedauthorized payment source has a sufficient balance or credit limit forthe monetary value that the user has requested for addition to thesmartcard 54.

If the authorized payment source has a sufficient balance or creditlimit, the “YES” branch is followed to step 3018, in which the debitcard Internet site adds the requested monetary value to the smartcard 54and charges the cost to the authorized payment source. Optionally, thedebit card Internet site may also load a rate schedule for services tobe provided by the meter 10 onto the smartcard 54. In this case, themeter 10 reads the monetary value assigned to performance of the testfrom the smartcard 54. Thus, rate schedules for various services to beperformed by the meter 10 may be changed from time to time, based onquantity discounts or other considerations. Step 3020 is followed by the“END” step, which concludes routine 3000.

Referring again to step 3016, if the payment source is invalid or doesnot have a sufficient balance or credit limit, the “NO” branch isfollowed to step 3017, in which the user is prompted for another paymentsource. If the user enters another payment source, the “YES” branchloops to step 3014 for validation of the alternate payment source. Ifthe user does not enter another payment source, the “NO” branch isfollowed by the “END” step, which concludes routine 3000.

FIG. 31 is a logic flow diagram illustrating a routine 3100 for using asmartcard 54 to pay for a service provided by the meter 10. In step3102, a user obtains a smartcard 54 with a usable monetary value,typically by purchasing a smartcard having a usable monetary value or byadding a monetary value to a smartcard as described with reference toFIG. 30. Step 3102 is followed by step 3104, in which the meter 10receives a request to provide a service, such as a blood cholesteroltest and/or production of a health report, with the associated cost tobe charged against a monetary value stored on the smartcard 54. Step3104 is followed by step 3106, in which the meter 10 prompts the user toenter a smartcard 54 with a usable monetary value into the meter. Step3106 is followed by step 3108, in which the meter 10 receives thesmartcard 54 in the reader 50. It should be understood that at thispoint the meter is inactive for performing services that requirepayment. Note also that the meter 10 may be activated alternativelythrough proprietary test strip validation, as described with referenceto FIG. 6.

Step 3110 is followed by step 3112, in which the meter 10 prompts theuser for a PIN for use with the smartcard 54 and validates the PIN(i.e., checks the received PIN against the PIN stored on the smartcard).If the PIN is validated, step 3112 is followed by step 3114, in whichthe meter 10 determines whether the monetary value stored on thesmartcard 54 is sufficient to pay for the requested service. As notedpreviously, the meter 10 may also read the rate schedule from thesmartcard 54. Alternatively, if no rate schedule is present on thesmartcard 54, the meter 10 may use a predefined “default” rate schedulefor the requested service.

If the monetary value stored on the smartcard 54 is sufficient to payfor the requested service, the “YES” branch is followed to step 3116, inwhich the meter 10 deducts the cost for the requested service from themonetary value stored on the smartcard 54. That is, the meter 10computes a revised monetary balance equal to the initial monetary valuestored on the smartcard less the cost for the requested service, andreplaces the initial monetary value stored on the smartcard with therevised monetary balance. Step 3116 is followed by step 3118, in whichthe meter 10 activates for performance of the requested service. Step3118 is followed by step 3120, in which the meter 10 completes therequested service and returns to the inactive state. Referring again tostep 3114, if the monetary value stored on the smartcard 54 isinsufficient to pay for the requested service, the “NO” branch isfollowed to step 3122, in which the meter displays a “balanceinsufficient” message. Steps 3120 and 3122 are followed by the “END”step, which concludes routine 3100.

The present invention thus provides a health monitoring and diagnosticdevice (LIFESTREAM cholesterol meter) that works in connection with anetwork-based comprehensive health analysis and reporting system. Theinvention also provides a secure medical records maintenance system thatworks in conjunction with the health monitoring and diagnostic device,and alternative business models for deploying the health monitoring anddiagnostic devices. It should be understood that the foregoing pertainsonly to the preferred embodiments of the present invention, and thatnumerous changes may be made to the embodiments described herein withoutdeparting from the spirit and scope of the invention.

The invention claimed is:
 1. A test medium for use with a healthmonitoring device, comprising: a test strip for receiving and carrying asample of biological fluid or tissue; the test strip carrying the sampleof biological fluid or tissue being readable by the health monitoringdevice to obtain test results based on the sample of biological tissueor fluid and calibration data specific to the test strip; the test stripcorresponding to a memory device readable by the health monitoringdevice, the memory device storing a code number and the calibrationdata; the test strip having an associated test strip identificationnumber that is mathematically derivable from the code number; the teststrip identification number being receivable by the health monitoringdevice through a user input device; and the test strip identificationnumber being usable to activate the health monitoring device for usewith the test strip only if the received test strip identificationnumber corresponds to a test strip identification number mathematicallyderived by the health monitoring device based on the code number readfrom the memory device.
 2. The test medium of claim 1, wherein: thememory device also stores an expiration date for the test strip; theexpiration date is readable by the health monitoring device; and theexpiration date is usable to activate the health monitoring device foruse with the test strip only if the expiration date is prior to acurrent date read by the health monitoring device from an internalclock.
 3. The test medium of claim 1, wherein the memory devicecomprises a romkey insertable into a socket housed within the healthmonitoring device.
 4. The test medium of claim 1, wherein: a pluralityof the test strips are packaged for distribution together with theromkey; and the test strip identification number is printed on the teststrips, printed on packaging for the test strips, or printed on a tagpackaged with the test strip.
 5. A hand-held health monitoring device,comprising: an enclosure for housing a disposable test strip for usewith the health monitoring device; a holder for removably supporting adevice for gathering a sample of biological fluid or tissue; a teststrip reader operable for reading the test strip carrying the sample ofbiological fluid or tissue and obtaining test results based on thesample of biological tissue or fluid and calibration data specific tothe test strip; a memory reading device functionally connected to thetest strip reader and operable for reading the calibration data from amemory device; a user input device operable for receiving user inputcommands; a display device operable for displaying information; aprocessor functionally connected to the test strip reader, the userinput device, and the display device, the processor containing a programmodule operable for obtaining the test results from the test stripreader and causing the display device to display the test results; and adata drive functionally connected to the processor and operable forwriting the test results to a removable memory storage device.
 6. Thehealth monitoring device of claim 5, wherein the processor is furtheroperable for: determining whether a personal identification number hasbeen previously stored on the removable memory storage device; if thepersonal identification number has not been previously stored on theremovable memory storage device prompting the user to enter a personalidentification number, storing the received personal identificationnumber on the removable memory storage device; and if the personalidentification number has been previously stored on the removable memorystorage device, prompting the user to enter a personal identificationnumber, comparing the stored personal identification number to thereceived personal identification number, and writing the test results tothe removable memory storage device only if the stored personalidentification number corresponds to the received personalidentification number.
 7. The hand-held health monitoring device ofclaim 5, further comprising: a clam-shell case openable to reveal firstand second compartments; the first compartment containing the enclosurefor housing the disposable test strip and the holder for removablysupporting the biological fluid or tissue gathering device; and thesecond compartment containing the test strip reader, the memory readingdevice, the display device, the processor, and the data drive.
 8. Thehand-held health monitoring device of claim 5, wherein: the biologicalfluid or tissue includes a droplet of human blood; and the test resultsinclude total cholesterol levels.
 9. The hand-held health monitoringdevice of claim 8, wherein the test strip reader is operable for readinga second type of test strip carrying a second sample of biological fluidor tissue and obtaining health-related test results based on the secondsample of biological tissue or fluid and calibration data specific tothe second type of test strip, further comprising: a second memoryreading device functionally connected to the test strip reader andoperable for reading calibration data from a second memory devicecorresponding to the second type of test strip.
 10. The hand-held healthmonitoring device of claim 9, wherein: the second biological fluid ortissue includes a droplet of human blood; and the test results includeblood glucose levels.
 11. A health monitoring device, comprising: a teststrip reader operable for reading the test strip carrying a sample ofbiological fluid or tissue and obtaining health-related test resultsbased on the sample of biological tissue or fluid and calibration dataspecific to the test strip; a memory reading device functionallyconnected to the test strip reader and operable for reading thecalibration data from a memory device; a user input device operationalfor receiving user input commands; a display device operable fordisplaying information; and a processor functionally connected to thetest strip reader, the user input device, and the display device, theprocessor containing a diagnostic program module operable for: obtainingthe test results from the test strip reader, causing the display deviceto prompt the user to enter diagnostic information using the user inputdevice, performing a diagnostic analysis to produce diagnostic resultsbased on the test results and the diagnostic information, and causingthe display device to display the diagnostic results.
 12. The healthmonitoring device of claim 11, wherein: the biological fluid or tissueincludes a droplet of human blood; the test results include blood lipidlevels; the diagnostic information includes one or more of the followingdata items corresponding to a person providing the droplet of humanblood: gender, ethnicity, family history of heart disease, personalhistory of heart disease, personal history of diabetes, personal historyof smoking, height, weight, age, blood pressure, fitness level; and thediagnostic results include one or more of the following data itemscorresponding to the person providing the droplet of human blood: amedical risk index, a recommended weight loss, a five-year risk of heartattack, a ten-year risk of heart attack, a cardiac age, an extended age,and a risk of stroke.
 13. The health monitoring device of claim 12,further comprising a data drive functionally connected to the processorand operable for writing the test results, the diagnostic information,and the diagnostic results to a removable memory storage device.
 14. Thehealth monitoring device of claim 13, wherein the processor is furtheroperable for: determining whether a personal identification number hasbeen previously stored on the removable memory storage device; if thepersonal identification number has not been previously stored on theremovable memory storage device prompting the user to enter a personalidentification number, storing the received personal identificationnumber on the removable memory storage device; and if the personalidentification number has been previously stored on the removable memorystorage device, prompting the user to enter a personal identificationnumber, comparing the stored personal identification number to thereceived personal identification number, and writing the test results,the diagnostic information, and the diagnostic results to the removablememory storage device only if the stored personal identification numbercorresponds to the received personal identification number.
 15. Thehealth monitoring device of claim 14, wherein the test strip reader isoperable for reading a second type of test strip carrying a secondsample of biological fluid or tissue and obtaining health-related testresults based on the second sample of biological tissue or fluid andcalibration data specific to the second type of test strip, furthercomprising: a second memory reading device functionally connected to thetest strip reader and operable for reading calibration data from asecond memory device corresponding to the second type of test strip. 16.The health monitoring device of claim 15, wherein: the second biologicalfluid or tissue includes a droplet of human blood; and the test resultsinclude blood glucose levels.